IMPPAT: Indian Medicinal Plants, Phytochemistry And Therapeutics
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IMPPAT Phytochemical information:
Nitidine
Summary
Physicochemical
Drug-likeness
ADMET
Descriptors
Summary
IMPPAT Phytochemical identifier:
IMPHY001258
Phytochemical name:
Nitidine
Synonymous chemical names:
nitidine
External chemical identifiers:
CID:4501
,
ChEMBL:CHEMBL176008
,
ChEBI:7578
,
ZINC:ZINC000000898732
,
FDASRS:933301178Z
,
SureChEMBL:SCHEMBL8014101
Chemical structure information
SMILES:
COc1cc2c[n+](C)c3c(c2cc1OC)ccc1c3cc2OCOc2c1
InChI:
InChI=1S/C21H18NO4/c1-22-10-13-7-17(23-2)18(24-3)8-15(13)14-5-4-12-6-19-20(26-11-25-19)9-16(12)21(14)22/h4-10H,11H2,1-3H3/q+1
InChIKey:
KKMPSGJPCCJYRV-UHFFFAOYSA-N
DeepSMILES:
COcccc[n+]C)ccc6cc%10OC)))))cccc6ccOCOc5c9
Functional groups:
c1cOCO1, cOC, c[n+](c)C
Molecular scaffolds
Scaffold Graph/Node/Bond level:
c1ccc2c(c1)c[nH+]c1c3cc4c(cc3ccc21)OCO4
Scaffold Graph/Node level:
C1CCC2C(C1)CNC1C3CC4OCOC4CC3CCC21
Scaffold Graph level:
C1CC2CC3CCC4C5CCCCC5CCC4C3CC2C1
Chemical classification
ClassyFire Kingdom:
Organic compounds
ClassyFire Superclass:
Organoheterocyclic compounds
ClassyFire Class:
Quinolines and derivatives
ClassyFire Subclass:
Benzoquinolines
NP Classifier Biosynthetic pathway:
Alkaloids
NP Classifier Superclass:
Tyrosine alkaloids
NP Classifier Class:
Isoquinoline alkaloids
NP-Likeness score:
0.866
Chemical structure download
2D:
2D MOL
2D MOL2
2D SDF
3D:
3D MOL
3D MOL2
3D SDF
3D PDB
3D PDBQT
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